Відео

Hi i wanna ask if How can you editing the genes of living creatures such as mice and others? If you do that, can you give me a link to the video?

I want to gene edit to make bomb ass espresso, can I have a kit? 😇😇

Is there any yes/no (qualitative) ELISA scenario for detecting a cancer biomarker using the Explorer Kit, or can only quantitative accurately simulate it?

May i ask you what did you major in university? i want to pursue a similar path to you but i am not sure what i should major in.

People talk about AGI yet we can't fully simulate one of these worms.

Background music please?

'Promosm' 🎶

pog

Hi Damon, this is a wonderful application for DNA barcoding. You do such a wonderful job!

Thanks sir

Thanks

Feel spread goodness

is this pseudomonas aeruginosa?

Good

Yoo thanks man, I was watching this for my Biomed class, explained perfectly!

I can editing in adults humaine

Whers i can do this technic ?

is there a continuation?

Sample buffer composition please

Nice video. may i ask you, so for this ouctherlony method what type of agar are you using in this test?

You can't open centrifuge tubes one handed like that, you're contaminating all of them.

Taking my AICE bio practical in two hours and spontaneously forgot how to do this. Thanks for the help!

🐝

goat

Thank you so much for the instructions.

I used this kit in my Microbiology class that I teach. Gives perfect results to teach Indirect ELISA assay. It uses a chicken gamma globulin for the antigen. Great simulation using real antigens and antibodies.

Thanks for the simple and educative video

Hey I’d like to make my pet hamster glow in the dark, can I get the kit?

The worm has entered the simulator!

🙂

좋아요!

Outstanding drawings!! Thank u for the lesson

Can you tell me which type of fish you used and the size of the protein? Thank you!

Thanks for the Video. What buffer did you use for casting the gel.

we flame the loop again and again can that flaming destroy our inoculum?

Hello, you forgot to include inverting the solution after you finished filling it to the etched line. Thanks for a great video otherwise!

Great video. Two notes: 1) the tone used during the discussion of eugenics is a bit too gleeful, and 2) the last passenger pigeon died at the Cincinnati zoo, not the Cleveland zoo.

Anything> 1.8 is pure DNA? I don't think so! Anything closer to 1.8 tells your DNA is pure! If close to 2 RNA contamination. If < 1.8, your DNA has some impurities (such as protein).

i hope this channel makes more videos on this topic

Do you have the viral titer to quantify?

Serious question.... What precautions have anyone taken for proper disposal of edited genes?

I live in Ethiopia. This kit will be used to teach students about the CRISPR/Cas9 gene-editing technology. Is it possible for me to obtain it? If so, from what source? Thank you for the interesting presentation.

superb.

Hi there, please help! I am conducting the antibacterial assay of my plant sample following the well diffusion method. But I have faced with a problem. Should I filter my plant sample with the help of 0.2 micron filter inside laminar flow cabinet before adding the samples into the wells. I found that when I filtered my sample, the concentration as well as the volume of my prepared sample also get decreased. I have also gone through severe literatures of my field but found no paper mentioning the use of 0.2 micron filter. So is it necessary to do so or I can skip this step?

Nice video

Brilliant video

What does the heat shock step do?

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